- Nearing the End of Life
- Your emotions as you near the end of life
- The importance of communication
- Making end-of-life decisions
- Advance directives
- Health care coverage
- Money and income
- Choosing home care
- Choosing hospice care
- Physical symptoms in the last 2 to 3 months of life
- When death is near
- Facing death
- To learn more
The importance of communication
Bill, age 65, with advanced cancer: “The doctors told me there was nothing else they could do for me except keep me comfortable. I felt like I wanted more say in what was going to happen next. They had offered me all they could; now I felt like I needed a little control. I wanted my family to suffer as little as possible and I wanted it to be as easy as it could be for them. I told the doctor I wanted him to be very honest with me about how long I had left. He told me he thought I had a few months. That was pretty much what I thought and I appreciated his honesty. It wasn’t his fault...”
With your health care team
Bill did what many cancer patients do at this stage of life. They choose to take more control and begin to actively plan the remaining part of their life.
Once the health care team says, “There are no more treatments that might cure your cancer,” the patient often thinks, “The ball is back in my court.” This is a healthy approach. Rather than being a passive recipient of care, you may now want to start thinking about how to help others accept and enjoy the time you have left. To do this, you need complete and honest information. Telling your doctor exactly what you want to know and getting the information you need are empowering steps. (In the section called “Making end-of-life decisions,” we will describe some ways for you to be sure that your wishes are followed, even if you become unable to communicate them.)
Making treatment decisions when facing the end of life
Some people aren’t willing to accept “no more treatment.” You may find that you want to get a second opinion and continue to actively fight the cancer. That’s OK! It’s your choice and you have to be comfortable with your decisions. Making your medical team and your loved ones part of the decision-making process will help things go more smoothly.
If you choose to have more treatment in spite of a doctor’s recommendations, explain your decision to those involved in your care. Even if they don’t understand or agree, you still must follow your own sense of what’s right for you. As long as you have fully explored all options, your friends and family will most likely support you. Keep in mind that no decision is forever. You can change your mind about treatment at any time.
On the other hand, you may prefer to spend your time focusing on the quality of your life. You may want to feel as well as you can without any more cancer treatments and side effects. Know that any symptoms you have can always be treated. Treatment of discomfort and pain is known as palliative or supportive care, and it’s different from treatment aimed at the cancer itself. When you decide you don’t want more cancer treatment, some family members may find it upsetting. Again, they will probably feel more supportive if they know that you’ve looked into all your options. You may want to share the reasons for your decision so they can better understand.
With your network of support
You may be someone who has never needed a large support network. Maybe it’s not easy for you to reach out to others, especially when you may feel you don’t have a lot to offer in return. Even so, there may be people in your life who want to support you through this time. They may be waiting for you to tell them what to do and how to help.
If friends and family are not available, there are often others who are. Online networks of support are also available, such as the American Cancer Society Cancer Survivors Network. Your local health care community may have support groups, and your religious community may have people who simply enjoy serving others. Hospice teams (which we will talk more about later) offer support resources for people with cancer.
It’s unrealistic, and maybe even unhealthy, to try to get through this time without supportive, loving people in your life. This is the time to reach out and enjoy people and the gifts they have to offer.
With your partner
Needs and demands
Cancer takes up a great deal of time and energy. Cancer and end-of-life care places a huge physical and emotional burden on those closest to you. Your partner may be either your greatest ally or a big disappointment as a source of support. There are obvious reasons for this. Your partner is probably dealing with his or her own emotions and yet feels a lot of pressure to come through for you and try to meet your every need. Some people just can’t handle that kind of pressure and may withdraw under these circumstances. They could pull away at a time when you feel you need them more than ever. This can be very painful.
On the other hand, your partner can be right there for you and that can be painful, too. It can be very troubling to know everything your partner is feeling and thinking and to see the pain they are going through. Sometimes partners try to protect each other from the pain they are both going through, but when this happens, honesty is sacrificed. Walls are built up, topics are avoided, and relationships can become strained and uncomfortable.
The death of a partner is one of the most stressful events a person can experience. Living with and anticipating this loss every day is even more stressful. If at all possible, try to talk with your partner about what each of you is feeling. You’ll probably find that you are both going through the same kinds of emotions. Try to accept what each person says without judgment, argument, or defending yourself. Simply let each person say what they feel. Don’t try to fix the feelings. Be aware of them and express your love and care for each other. This is another chance to try to make any past wrongs right and comfort each other. But having cancer doesn’t mean that you won’t get angry and frustrated with each other. Try to focus on the comfort you can give each other and let petty arguments go. Focus on the good times, happy memories, and the times you have been there for each other.
It’s also important to allow each other personal space and private time. Reassure each other that you still love each other, but it’s OK if you both need some time to be alone. This is a common need as a person faces the end of life. No one can be with someone 24 hours a day. And you cannot squeeze a lifetime into a few months. Make the most of each day, be grateful for it, and greet the next one as a new chance to enjoy each other.
Sex and intimacy
At this stage of your illness it may be hard to be as sexually close as you have been in the past. You may be tired, in some pain, or simply not interested in sex. But you can still keep physical contact in your relationship and share intimacy. Talk with your partner about your needs. Tell him or her that you want to be close but that you don’t feel you are able to have sex. Make sure your partner understands you want physical closeness and affection. At this time simply touching, hugging, and holding hands may feel more intimate than other forms of physical contact.
Help take care of your partner
You may need to talk to your partner if you’re worried about being a burden to them because they are taking care of you. Ask how he or she is managing it. Your partner may show signs of emotional and physical stress, such as depression, headaches, trouble sleeping, or weight loss or gain. Remind your partner to take care of him or herself. Ask a friend or another family member to help out if you think there’s too much for one person to do. Be sure to tell your partner you are going to do that. In this way, you can help take care of your partner, too.
With your family
Cancer is a family illness. Your loved ones are hurting too. Each member of your family is working through his or her own emotional responses to the idea of losing you. They need your love and understanding. Though it might seem impossible, there are things you can do to help them manage better.
You can help adult family members by being open about your disease process, the amount of time you’ve been told you have left, and any other needs you may have. It also helps to share with them the expected signs of the dying process, and how to manage them should they occur. Explain to your family that you’re open to discussion and that you’re willing to talk about anything. Explore their thoughts and feelings with them. Tell them that you are open to talking, but there may be times you don’t feel like it and you will let them know when that is. Tell them that you’d rather not try to put on an act and have to pretend you’re happy if you don’t feel happy. Explain to them this doesn’t mean you aren’t OK. It may just mean you are feeling tired or a little down.
Tell your family that you will be as honest with them as you can be and would like the same from them in return. Give them information about what you expect to happen in the future so they’ll be prepared. Tell them about plans you’ve made or need to make and get their input. Adult children may be juggling their own children, jobs, and caring for you. It’s a stressful time. Sometimes they might not be able to meet your expectations. Open, honest communication will help you support each other through this time.
Children and teens
It’s natural to want to protect children from the harsh reality that you won’t be there in a few months. But professionals who work with families would strongly encourage you not to try that. Even the youngest need some type of preparation for the future. Honesty is important. Children can usually sense changes or stress in the household and know when something is wrong. Many times what they imagine is far worse than anything you have to tell them.
Children naturally focus mainly on themselves. And they often think they caused the problems they sense in those around them. They might even believe that something they’ve done caused the cancer to grow. It’s up to you to assure them that they had nothing to do with your cancer, its growth, or with the fact that you will not win your battle against it. Let them know that you’ll keep fighting, but the doctors have given you all the treatments they can.
Tell them you want to share some good times with them before the cancer takes over. Children also need to know what plans will be in place when you’re no longer there. Explain in some detail what will happen when you’re gone; how they will be cared for and by whom. If the child is mature enough, tell them that you will always be in their heart even if your body is not around. This will be a hard discussion. It’s sad for you and for them, but they need to know these things. Tell your child that no topic is off limits. They can talk to you about or ask you anything they want.
Sometimes it helps to tell your kids about people and places they can go to when they’re sad. Encourage your children to talk about their feelings. Make sure they know that you would consider it normal, and even helpful, if they had counseling or were in a support group to help them through this time. Encourage your child to help you with some physical tasks, such as getting things for you or reading books to you. This way they don’t feel so helpless or in the way. It’s easy for busy adults to ignore or push kids out of the way without meaning to do so. Don’t allow your child to feel devalued at such a critical time. These moments with your child are precious. They will become fond memories they can cherish in the future. For more on talking with children and teens, see Helping Children When a Family Member Has Cancer: Dealing With a Parent’s Terminal Illness.
With your friends
Some friends respond as you would expect them to – they are warm, supportive, and available. Other friends may seem to be more awkward around you. They may act as if they don’t know what to say or do and seem to have a hard time being “normal.” Sometimes you can talk to your friends about their discomfort. Explain that you’re the same person and you’d like to spend some of your remaining time with them, if they are willing to do that. Try to understand that what you’re going through may cause your loved ones to think about the fact that they, too, will die. Because this is not a pleasant thing to think about, some people may avoid spending time with you.
With support groups
Taking part in a group can give you sense of belonging. It also gives you a safe place to talk about fears and emotions that you may feel uncomfortable talking about with other people. Group involvement has been shown to ease isolation and reduce stress.
There are many types of support groups, both formal and informal. Some formal groups are set up for caregivers, others for people with certain types of cancers, or people of certain ages. There are bereavement groups for adults and even some for children who have lost a loved one to cancer. In a support group, you are with people who are coping with the same problems and issues that you are facing. The encouragement and understanding found in a group of people sharing a critical life experience can be very valuable. Groups may only last a given number of weeks or months, or they may be open ended.
You may find it hard to go out to meetings in your last weeks of life. Some of the more informal groups, such as a neighborhood group of friends or a church group, may be willing to come to your home. Internet support groups may be a good option for people who are homebound and able to use a computer. Often hospice organizations are involved in the last months of life and they offer the help of staff members who can give specific types of support around specific needs. For example, there are staff members who talk about emotional support. There are also those who focus on spiritual concerns. Clergy or other spiritual leaders are often willing to make home visits to people in the last months of life.
You can get information on available support groups from your medical team, your facility or hospice social worker, or from your American Cancer Society.
Last Medical Review: 01/14/2014
Last Revised: 02/06/2014